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无管微流控血管生成分析检测方法,结合了三维内皮衬里微血管。

Tubeless microfluidic angiogenesis assay with three-dimensional endothelial-lined microvessels.

机构信息

Department of Biomedical Engineering, University of Wisconsin-Madison, Madison, WI 53706, USA.

出版信息

Biomaterials. 2013 Feb;34(5):1471-7. doi: 10.1016/j.biomaterials.2012.11.005. Epub 2012 Nov 26.

Abstract

The study of angiogenesis is important to understanding a variety of human pathologies including cancer, cardiovascular and inflammatory diseases. In vivo angiogenesis assays can be costly and time-consuming, limiting their application in high-throughput studies. While traditional in vitro assays may overcome these limitations, they lack the ability to accurately recapitulate the main elements of the tissue microenvironment found in vivo, thereby limiting our ability to draw physiologically relevant biological conclusions. To bridge the gap between in vivo and in vitro angiogenesis assays, several microfluidic methods have been developed to generate in vitro assays that incorporate blood vessel models with physiologically relevant three-dimensional (3D) lumen structures. However, these models have not seen widespread adoption, which can be partially attributed to the difficulty in fabricating these structures. Here, we present a simple, accessible method that takes advantage of basic fluidic principles to create 3D lumens with circular cross-sectional geometries through ECM hydrogels that are lined with endothelial monolayers to mimic the structure of blood vessels in vitro. This technique can be used to pattern endothelial cell-lined lumens in different microchannel geometries, enabling increased flexibility for a variety of studies. We demonstrate the implementation and application of this technique to the study of angiogenesis in a physiologically relevant in vitro setting.

摘要

血管生成的研究对于理解包括癌症、心血管和炎症性疾病在内的多种人类病理生理学非常重要。体内血管生成测定法可能既昂贵又耗时,限制了它们在高通量研究中的应用。虽然传统的体外测定法可能克服这些限制,但它们缺乏准确重现体内组织微环境的主要元素的能力,从而限制了我们得出生理相关生物学结论的能力。为了弥合体内和体外血管生成测定法之间的差距,已经开发了几种微流控方法来生成体外测定法,该方法将具有生理相关三维(3D)管腔结构的血管模型与体外测定法相结合。然而,这些模型并没有得到广泛采用,这在一定程度上可以归因于制造这些结构的困难。在这里,我们提出了一种简单、可及的方法,该方法利用基本的流体原理,通过 ECM 水凝胶创建具有圆形横截面几何形状的 3D 管腔,该水凝胶内衬有内皮单层细胞,以模拟体内血管的结构。该技术可用于对不同微通道几何形状的内皮细胞衬里管腔进行图案化,为各种研究提供更大的灵活性。我们展示了该技术在生理相关体外环境中血管生成研究中的实施和应用。

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